ENST00000223051.8:c.2210G>T
MANE Select
|
ENSP00000223051.3:p.Gly737Val
|
|
ENST00000223051.7:c.2210G>T
|
ENSP00000223051.3:p.Gly737Val
|
|
ENST00000431692.5:c.*885G>T
|
ENSP00000413905.1:n.*885G>T
|
|
ENST00000462090.5:n.1246G>T
|
|
|
ENST00000462107.1:c.2210G>T
|
ENSP00000420525.1:p.Gly737Val
|
|
ENST00000465294.5:n.2130G>T
|
|
|
ENST00000476304.5:n.1831G>T
|
|
|
ENST00000490084.5:c.1563G>T
|
|
|
NM_001206855.1:c.1697G>T
|
NP_001193784.1:p.Gly566Val
|
|
NM_003227.3:c.2210G>T
|
NP_003218.2:p.Gly737Val
|
|
XM_005250553.3:c.2210G>T
|
XP_005250610.1:p.Gly737Val
|
|
NM_001206855.2:c.1697G>T
|
NP_001193784.1:p.Gly566Val
|
|
XM_005250553.4:c.2210G>T
|
XP_005250610.1:p.Gly737Val
|
|
XM_017012573.1:c.2210G>T
|
XP_016868062.1:p.Gly737Val
|
|
NM_003227.4:c.2210G>T
MANE Select
|
NP_003218.2:p.Gly737Val
|
|
NM_001206855.3:c.1697G>T
|
NP_001193784.1:p.Gly566Val
|
|